Laparoscopic Revision of Jejunoileal Bypass to Gastric Bypass (JIB-to-RYGB)
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|ClinicalTrials.gov Identifier: NCT01040533|
Recruitment Status : Completed
First Posted : December 29, 2009
Last Update Posted : December 29, 2009
This study objectives are the following.
- To describe the updated clinical presentation, indications, and multidisciplinary medical management of patients with a failed and/or complicated jejunoileal bypass (JIB).
- To analyze the feasibility, safety, and efficacy of one-stage laparoscopic re-operative gastric bypass surgery for failed and/or complicated Jejunoileal bypass (JIB) for weight loss.
- To determine what factors or strategies are associated with a successful outcome. In particular, the completion of the surgery in one stage with a laparoscopic approach.
|Condition or disease|
|Clinically Severe Obesity Metabolic Complications After Jejunoileal Bypass Nutritional Complications After Jejunoileal Bypass Obesity Recidivism Inadequate Initial Weight Loss Intestinal Malabsorptive Syndrome Protein Malnutrition|
Show Detailed Description
|Study Type :||Observational|
|Actual Enrollment :||4 participants|
|Official Title:||One-stage Laparoscopic Revision of Failed and/or Complicated Jejunoileal Bypass to Roux-en-Y Gastric Bypass|
|Study Start Date :||December 2008|
|Primary Completion Date :||December 2009|
|Study Completion Date :||December 2009|
|Failed / complicated jejunoileal bypass|
- Morbidity and mortality [ Time Frame: throughout follow-up ]
- Weight loss expressed as Body Mass Index and Percentage excess weight loss [ Time Frame: throughout follow-up ]
- Remission or improvement of symptoms and JIB-related complications [ Time Frame: throughout follow-up ]
- Remission or improvement of other comorbidities [ Time Frame: throughout follow-up ]
- Operative time [ Time Frame: transoperatively ]
- conversion to open approach [ Time Frame: transoperatively ]
- Hospital stay [ Time Frame: same hospitalization ]
To learn more about this study, you or your doctor may contact the study research staff using the contact information provided by the sponsor.
Please refer to this study by its ClinicalTrials.gov identifier (NCT number): NCT01040533
|United States, California|
|UCSF Fresno Center for Medical Education and Research, Department of Surgery|
|Fresno, California, United States, 93701|
|Study Director:||Francisco M Tercero, MD||Research Associate, University of California San Francisco|
|Principal Investigator:||Kelvin D Higa, MD||Professor of Surgery, University of California San Francisco|